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Is there a justification for classifying GLP-1 receptor agonists as basal and prandial

In the STEP UP trial, only 5.4% of patients stopped treatment due to side effects

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Due to the concern about the growing prevalence of unapproved GLP-1s on the market, the FDA issued warning letters to the following companies in December: The FDA warned the companies about potential violations of the Federal Food, Drug, and Cosmetic Act (FD&C Act), even with the companies claiming some of their GLP-1 products were currently for research purposes only

GLP-1 Receptor Agonist is a research-grade single-pathway incretin peptide supplied in lyophilized vial format for controlled laboratory work examining single-pathway incretin receptor signaling and comparative peptide-pathway models